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Copyright: ©Author(s) 2026.
World J Gastrointest Surg. Nov 27, 2026; 18(11): 125637
Published online Nov 27, 2026. doi: 10.4240/wjgs.125637
Table 1 Diagnostic performance, heterogeneity and risk of bias of emergency point-of-care ultrasound applications in the acute abdomen
Ref.
Population/setting
Operator
Reference standard
Diagnostic threshold
Sensitivity (95%CI)
Specificity (95%CI)
LR+/LR-
Studies/patients
Heterogeneity (%)
Risk of bias/certainty
Interpretation and limitations
SBO: Study-level meta-analysis (Gottlieb et al[9], 2018)ED and inpatient adults with suspected SBOMixed (EP and others)CT, surgery, or final diagnosisDilated loop > 25 mm92.4% (89.0%-94.7%)96.6% (88.4%-99.1%)27.5/0.0811/1178NR in retrievable textQUADAS-2 not reported in retrievable text; no GRADEStrong rule-in; study-level pooling may overestimate sensitivity
SBO: IPD meta-analysis (Shokoohi et al[10], 2023)Multicentre ED, adultsEP (attending and resident)CT/surgery/final diagnosisDilated loop > 25 mm83.0% (71.7%-90.4%)93.0% (55.3%-99.3%)11.9 (1.2-114.9)/0.25/433NR in retrievable textIPD design reduces reporting bias; no GRADEMost conservative estimate; specificity CI so wide the parameter is effectively unestimated
SBO: Meta-analysis with QUADAS-2 (Motavaselian et al[30], 2024)ED adults with suspected SBOMixedCT/surgery/final diagnosisDilated loop > 25 mmNR here (see source)0.80 (0.77-0.83)N/A21/197762% sensitivity; 88% specificity (both P < 0.01)QUADAS-2: High risk for patient selection and flow/timing in several studies; Egger P = 0.04Specificity 16 points below the two estimates above; publication bias detected
SBO: Bedside-threshold analysis (Shokoohi et al[11], 2024)ED adultsEPCT/surgeryLoop > 2.75 cm (AUC = 0.76, 0.71-0.81); ≤ 1.7 cm 100% sensitivity; > 4 cmN/AApproximately 90.7% at > 4 cmN/AIPD secondary analysisN/AUnvalidated threshold-derivation studyCandidate threshold only; no measurement convention specified; age/sex shift optimum (2.95 cm at ≥ 65 years)
Acute cholecystitis: EP-POCUS meta-analysis (Wilson et al[32], 2024)ED adults, suspected acute cholecystitisEPFinal diagnosisStones + wall > 3 mm + Murphy sign + pericholecystic fluid70.9% (62.3%-78.2%)94.4% (88.2%-97.5%)12.7/0.3110 included; estimates from 7/1772NR in retrievable textNot reported in retrievable textRule-in test; negative scan does not exclude
Acute cholecystitis: All-operator meta-analysis (Huang et al[25], 2023)Mixed settings, all specialties (EP subgroup)All operators; EP subgroupFinal diagnosis/pathologyAs above71% (69%-72%); EP 71% (67%-74%)85% (84%-86%); EP 92% (90%-93%)N/A40/865289.7% (87%-92%)QUADAS-2: > 25% of studies high risk (case-control design, non-consecutive enrolment)Operator specialty changes specificity by 7 points
Acute cholecystitis: Prospective TG18-adjudicated cohort (Nipitkul et al[33], 2026)ED adults, high disease prevalenceEPTG18POCUS criteria vs TG18 (wall > 3 mm vs ≥ 4 mm scales)86.6% (83.4%-89.4%)17.1% (12.5-22.5)NR/NPV 37.0%1/783N/A (primary study)Prospective; single reference standardDiscordant with pooled specificity of 85%-94%; only gallstones were significantly associated with confirmed disease
Gastric: ED intubation cohort (Asokan et al[27], 2023)ED adults undergoing urgent intubationEPAspiration-relevant gastric contentAntral CSA ≥ 9.27 cm²100%87%N/A1/100N/ASingle-centreRisk stratification against a surrogate endpoint, not diagnosis
Gastric: Fasting IPD meta-analysis (Perlas et al[26], 2024)Fasting adults (reference range)Trained sonographersEndoscopic/measured volume95th-percentile CSA 9.9 cm² (9.4-10.4); volume 2.3 mL/kg (2.3-2.4)Grade 0/1 → 98% probability below thresholdN/AN/A12/1203NR in retrievable textReference-range derivationThresholds do not generalise across position or population
Free fluid: Ectopic pregnancy (Moore et al[31], 2007)ED women, suspected ectopic pregnancyEPOperative interventionAny free fluid in Morison's pouchN/AN/ALR+ 112 (15-831)1/242N/ASingle-centre; estimate rests on 10 fluid-positive patientsDecisive rule-in in a high-pretest obstetric population only
Free fluid: Prehospital FAST meta-analysis (Lin et al[19], 2024)Prehospital traumaPrehospital providersCT/laparotomyAny free fluid0.596 (0.345-0.822)0.970 (0.953-0.983)N/A6/135694%aGRADE: Sensitivity very low (inconsistency, imprecision, publication bias); specificity highTrauma population, indirect evidence for non-traumatic disease; indicates the sensitivity ceiling
Free fluid: Cochrane review, blunt trauma (Stengel et al[18], 2018)Blunt thoracoabdominal trauma, adults and childrenMixedCT/laparotomy/clinical follow-upAny free fluid0.74 (0.65-0.81); children 0.63 (0.46-0.77)0.96 (0.94-0.98)N/A34 studiesReported in sourceCochrane methodologyAt 28% prevalence, 73 injured adults and 118 injured children missed per 1000 scanned
Appendicitis: POCUS meta-analysis (Matthew Fields et al[35], 2017)ED adults and childrenNon-radiologist physicians; EP subgroupPathology/final diagnosisNon-compressible, dilated appendix91% (83%-96%); EP subgroup 80%97% (91%-99%); EP subgroup 92%N/A21/NR99% (99%-100%)Not reported in retrievable textExtreme heterogeneity; EP-only performance lower than the headline figure
Appendicitis: Paediatric meta-analysis (Miller et al[36], 2026)ChildrenMixedPathology/final diagnosisNon-compressible, dilated appendix85.6% (68.9%-94.1%)90.2%N/A8/993Sensitivity range 53%-100% across studiesRecent; see sourceBetween-study range wider than the pooled CI implies
Hydronephrosis/renal colic (Wong et al[37], 2018)ED adults, suspected renal colicEPCTAny hydronephrosis70.2% (67.1%-73.2%)N/AN/ANR in retrievable textNR in retrievable textNot reported in retrievable textRisk stratification only; cannot exclude
AAA (Shaban et al[34], 2025)ED adults, symptomaticEPCT/operative/final diagnosisAortic diameter ≥ 3 cm (aneurysm definition)98.33%99.84%N/A9/NRNR in retrievable textNot reported in retrievable textIdentifies an aneurysmal aorta; does NOT identify rupture, for which CT angiography is the reference standard
Table 2 Tokyo Guidelines 2018 diagnostic and severity criteria relevant to bedside sonography
Item
Acute cholecystitis
Acute cholangitis
Diagnostic criteriaOne local sign of inflammation + one systemic sign = suspected; + characteristic imaging = definite[21]One item of systemic inflammation + one item of cholestasis or imaging = suspected; all three = definite[88]
Systemic inflammationN/AFever > 38 °C, or laboratory evidence of an inflammatory response[88]
CholestasisN/AJaundice with total bilirubin ≥ 2 mg/dL, or liver function tests > 1.5 × upper limit of normal[88]
Imaging itemCharacteristic imaging findings (wall thickening ≥ 4 mm among them)[21]Biliary dilatation, or evidence of aetiology (stricture, stone, stent)[88]
Grade I (mild)No organ dysfunction; mild local inflammatory change[21]Neither grade II nor grade III criteria met[88]
Grade II (moderate)Any one of: WBC > 18000/mm³; palpable tender RUQ mass; complaints > 72 hours; marked local inflammation (gangrenous or emphysematous cholecystitis, pericholecystic or hepatic abscess, biliary peritonitis)[21]Any two of five criteria, one of which is age ≥ 75 years[88]
Grade III (severe)Dysfunction of any one organ system: Cardiovascular (hypotension requiring dopamine ≥ 5 μg/kg per minute, or any dose of noradrenaline); neurological (decreased consciousness); respiratory (PaO2/FiO2 < 300); renal (oliguria or creatinine > 2.0 mg/dL); hepatic (PT-INR > 1.5); haematological (platelets < 100000/mm³)[21]Organ dysfunction as for cholecystitis[88]
Management by gradeGrade I and grade II (experienced surgeons): Early laparoscopic cholecystectomy where CCI ≤ 5 and ASA-PS ≤ 2; otherwise, medical treatment and/or gallbladder drainage with interval cholecystectomy. Grade III: Early or urgent biliary drainage with delayed cholecystectomy; upfront surgery only with favourable organ-system failure, no negative predictive factors, CCI ≤ 3, ASA-PS ≤ 2, in an advanced centre[81]Biliary drainage, urgently in severe disease[88]
Sonographic component of gradingNone: Grading uses vital signs, organ-failure laboratory values, WBC, symptom duration and comorbidity indices[21]None[88]
Table 3 The authors’ proposed specification: What a consensus process would need to fix before these applications can be standardised
Consensus item
SBO
Gastric assessment
Free fluid beyond trauma
Biliary tract
Minimum image setNumber of quadrants required for a complete study is undefined; segmental obstruction means an incomplete survey can be falsely negative. Fix: Mandated quadrants and documented images per quadrantSupine and RLD antral views are used inconsistently; some thresholds are supine-derived and others RLD-derived. Fix: Both positions mandatory, each documentedNumber and identity of dependent recesses varies outside the FAST protocol; pelvic views may be omitted in non-trauma scanning. Fix: Defined recess set for the non-traumatic indicationLong-axis and short-axis gallbladder views, wall measurement site and duct view are not standardised. Fix: Mandated views including the point of wall measurement
Measurement conventionNo published convention specifies outer-to-outer vs inner-to-inner, plane, or whether maximal or averaged loop diameter is used, a difference capable of exceeding the 2.5 mm separating the 2.5 cm and 2.75 cm thresholds. Fix: Single defined conventionAntral CSA is derived by different formulae and at different antral levels. Fix: One formula, one anatomical level, one patient position per stated thresholdVolume estimation and the distinction between trace, small, moderate and large collections are undefined; agreement falls to kappa 0.48-0.65 for this distinction. Fix: Defined volume categories with anchoring imagesWall thickness is measured at unspecified sites and on discordant scales, > 3 mm in the emergency literature against ≥ 4 mm in TG18. Fix: One threshold, one measurement site, one wall (anterior)
Definition of a positive studyWhether dilatation alone suffices, or dilatation plus abnormal peristalsis, or plus interloop fluid, varies between studies. Fix: Explicit rule for the compositeA positive study means different target volumes in different sources (empty stomach, > 1.25 mL/kg, aspiration-relevant content). Fix: State the target volume with the thresholdAny anechoic fluid vs a clinically significant volume is not distinguished. Fix: Population-specific definition, since physiological pelvic fluid differs by sex and pregnancy statusNumber and combination of signs required is unstated; agreement is kappa 0.85 for gallstones but 0.37 for the composite diagnosis. Fix: Defined minimum criteria set, aligned to TG18
Reporting lexiconTerms for peristaltic patterns and the valvulae sign are used inconsistently across the literature. Fix: Controlled vocabulary with defined termsPerlas grades 0-2 are well defined but quantitative and qualitative results are reported interchangeably. Fix: Report grade and CSA separately, never as equivalentsDescriptors of volume and location vary. Fix: Standardised recess names and volume categoriesSonographic Murphy sign has no standardised elicitation, defined transducer pressure or accounting for prior analgesia. Fix: Defined elicitation protocol, or removal of the sign from criteria
Reference standardCT, surgical findings and final clinical diagnosis are used interchangeably across pooled studies. Fix: Single specified standard, or pre-specified stratification by standardAspirated volume, endoscopic volume and model-predicted volume are used as equivalents. Fix: One standard; and outcome studies linking measurement to aspiration rather than to volumeTrauma-derived standards (CT, laparotomy) are applied to non-traumatic populations. Fix: Indication-specific reference standardFinal diagnosis, pathology and TG18 give materially different specificity (17.1% vs 85%-94%). Fix: TG18 as the uniform standard, with the index test measured on the same scale
Training volume for credentialingNo application-specific minimum; the attending-resident sensitivity gap is 14.7 percentage points. Fix: Application-specific case minimum with competency assessmentNo emergency-setting training standard exists; the available reliability study used three raters and healthy volunteers. Fix: Defined supervised case volumeFAST credentialing exists but is trauma-specific and does not cover non-traumatic indications. Fix: Extension of credentialing to the non-traumatic indicationCredentialing exists in most curricula but is not tied to demonstrated agreement on wall thickness or the Murphy sign. Fix: Competency demonstrated per sign, not per application
Quality assuranceNo archived-image review requirement; loop measurement cannot be audited if images are not stored. Fix: Mandatory archiving of the measured loopNo QA mechanism described in any cited source. Fix: Archived antral images with periodic measurement auditWhere archiving exists it is trauma-oriented. Fix: QA review of non-traumatic studies, with attention to small collectionsQA review is described in stewardship literature but is not sign-specific. Fix: Periodic audit of wall measurement and of Murphy-sign documentation
Priority reliability studies requiredInter-observer agreement for loop-diameter measurement: No published kappa or ICC was identified for this measurement, on which the entire branch turnsInter-observer agreement for antral CSA in an emergency population; and any study linking measurement to aspiration rather than to volumeInter-observer agreement for detecting a small collection in a non-traumatic emergency population, none identifiedInter-observer agreement for millimetre wall-thickness measurement in an emergency setting (none identified) and a second, multicentre study of the sonographic Murphy sign
Table 4 Evidence-versus-proposal matrix for each action node of the integrated algorithm (Figure 1): What the node rests on, and whether it is derived from evidence or proposed by the authors
Algorithm action node
Evidence type
Evidence supporting the node
Status
Ref.
Step 1: Instability/red-flag check precedes any scanExpert recommendationConsensus statements on emergency POCUS scope; no comparative trial of scan-first vs resuscitate-firstAuthors’ proposalKameda and Taniguchi[7], Oto et al[8]
Step 2: Operator competency preconditionEvidence-informedOperator-level subgroup estimates differ by application and do not all run the same way: For appendicitis the EP subgroup is lower than the pooled estimate on both axes (sensitivity 80% vs 91%, specificity 92% vs 97%), whereas for cholecystitis the EP subgroup matches the pooled sensitivity (71% vs 71%) and exceeds the pooled specificity (92% vs 85%). Competency is therefore required as a precondition because performance is operator-dependent in an application-specific direction, not because EP performance is uniformly lowerEvidence-based (subgroup estimates), authors’ proposal (credentialling requirement)Huang et al[25], Matthew Fields et al[35]
Step 3: Symptom cluster sets pretest probability and orders the scansAuthors’ constructionNo study compares symptom-ordered POCUS sequencing against a fixed protocolAuthors’ proposalN/A
Biliary branch: Gallstones + sonographic Murphy sign + wall > 3 mm as the rule-in triggerEvidence-basedPooled specificity 94.4% (88.2%-97.5%) for EP-performed POCUS; TG18 uses wall ≥ 4 mmEvidence-basedYokoe et al[21], Wilson et al[32]
Biliary branch: Negative scan does not exclude cholecystitisEvidence-basedPooled EP sensitivity 70.9% (62.3%-78.2%); LR- accordingly poorEvidence-basedWilson et al[32]
Biliary branch; fever + jaundice + dilated duct triggers the cholangitis pathwayGuideline-basedTG18 diagnostic criteria (systemic inflammation + cholestasis + imaging) and severity gradingEvidence-based (guideline)Okamoto et al[81], Kiriyama et al[88]
SBO branch: Dilated loops > 2.5 cm as the rule-in triggerEvidence-basedPooled sensitivity 92.4% (89.0%-94.7%), specificity 96.6% (88.4%-99.1%), LR+ 27.5Evidence-basedGottlieb et al[9]
SBO branch: 2.75 cm as a candidate refined thresholdAuthors’ constructionProposed in a bedside-threshold analysis; no reliability data exist for bowel-loop diameter at this precisionAuthors’ proposal: Explicitly unvalidatedShokoohi et al[11]
SBO branch, CT still required for transition point, aetiology, ischaemia, perforationEvidence-basedConsistent statement across the SBO syntheses; POCUS not evaluated for these endpointsEvidence-basedGottlieb et al[9], Shokoohi et al[10], Motavaselian et al[30]
Free-fluid branch, free fluid in Morison’s pouch or pelvis as the rule-in triggerEvidence-basedEctopic pregnancy cohort; prehospital FAST pooled specificity 0.970 (0.953-0.983)Evidence-basedLin et al[19], Moore et al[31]
Free-fluid branch: Ectopic pregnancy excluded only by seeing an intrauterine pregnancyEvidence-basedPooled FAST sensitivity 0.74 (0.65-0.81) in blunt trauma; absent free fluid carries no exclusionary value for ectopic pregnancyEvidence-basedStengel et al[18], Moore et al[31]
Aorta/renal branch, aortic diameter ≥ 3 cm; POCUS does not identify ruptureEvidence-basedAneurysm detection sensitivity 98.3%, specificity 99.8%; no pooled estimate for rupture detectionEvidence-basedShaban et al[34]
Gastric parallel branch: Perlas grade and antral CSA stratify aspiration riskEvidence-basedIPD meta-analysis: Grade 0/1 gives 98% probability of being below the risk threshold; ED intubation cohort sensitivity 100%, specificity 87%Evidence-based (against a surrogate endpoint)Perlas et al[26], Asokan et al[27]
Gastric parallel branch; thresholds are position- and population-specific, not interchangeableEvidence-basedDistinct CSA thresholds by position and population across the source studiesEvidence-basedPerlas et al[26]
Third exit; non-diagnostic study treated separately from a negative studyAuthors’ constructionNo source study reports a distinct action pathway for non-diagnostic examinationsAuthors’ proposal, a principal original contributionN/A
Serial scanning after an interval where the picture is evolvingExpert recommendationNo comparative evidence for serial abdominal POCUS in this settingAuthors’ proposalN/A
Secondary redirect applications when the entry scan is negative or non-diagnosticEvidence-based (component estimates), authors’ construction (the redirect rule)Appendicitis EP sensitivity 80%, specificity 92%; hydronephrosis sensitivity 70.2%; AAA detection 98.3%Mixed, estimates evidence-based, sequencing proposedShaban et al[34], Matthew Fields et al[35], Miller et al[36], Wong et al[37]
Governing principle, every application rules in better than it rules outEvidence-basedDirect consequence of the sensitivity/specificity asymmetry documented in Table 1Evidence-basedGottlieb et al[9], Shokoohi et al[10], Stengel et al[18], Lin et al[19], Huang et al[25], Wilson et al[32]


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